Department of Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Curr Drug Targets. 2010 Jun;11(6):652-66. doi: 10.2174/138945010791170923.
Indole compounds, obtained from cruciferous vegetables, have been investigated for their putative anti-cancer properties. Studies with indole-3-carbinol (I3C) and its dimeric product, 3, 3' diindolylmethane (DIM), have indicated efficacy of these compounds against a number of human cancers. Available as well as emerging data suggests that these compounds act on a number of cellular signaling pathways leading to their observed biological effects. Such pleiotropic effects of these compounds are also considered crucial for their chemosensitization activity wherein they help reduce the toxicity and resistance against conventional chemotherapeutic drugs. These observations have major clinical implications especially in chemotherapy. Through this review, we have attempted to update current understanding on the state of anti-cancer research involving indole compounds. We have also summarized the available literature on modulatory effects of indoles on molecular targets such as survivin, uPA/uPAR and signaling pathways such as the NF-kappaB pathway, which are important for the apoptosis-inducing and chemosensitizing properties of these compounds.
吲哚类化合物来源于十字花科蔬菜,因其潜在的抗癌特性而受到研究。吲哚-3-甲醇(I3C)及其二聚产物 3,3' 二吲哚甲烷(DIM)的研究表明,这些化合物对多种人类癌症具有疗效。现有和新兴的数据表明,这些化合物作用于多种细胞信号通路,从而产生其观察到的生物学效应。这些化合物的这种多效性作用也被认为对其化学增敏活性至关重要,因为它们有助于降低传统化疗药物的毒性和耐药性。这些观察结果在化疗中具有重要的临床意义。通过这篇综述,我们试图更新涉及吲哚化合物的抗癌研究的最新认识。我们还总结了关于吲哚类化合物对分子靶点(如生存素、uPA/uPAR)和信号通路(如 NF-κB 通路)的调节作用的现有文献,这些靶点和信号通路对这些化合物的诱导凋亡和化学增敏特性很重要。